Metabolism Flashcards

1
Q

The low activity of insulin in type 1 diabetes results in what metabolic effects?

A

Catabolic actions of glucagon are unopposed

Breakdown of carbohydrate, protein and fat

Hyperglycaemia, ketoacidosis, hypertriglyceridaemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Differences in the effects starvation and type 1 diabetes?

A

Type 1 diabetes has absent insulin, in starvation there is still a small amount

In starvation blood glucose is maintained, but in diabetes there is hyperglycaemia

In Type 1 diabetes there is much more ketone formation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Time course of type 2 diabetes?

A

Early: plasma glucose normal despite insulin resistance as B cells can compensate

B cells eventually cannot compensate leading to impaired glucose tolerance and inflammation

Insulin resistance and impaired secretion lead to a failure to suppress gluconeogenesis at all and there is fasting hyperglycaemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Difference in metabolic effects in Type 1 and 2 diabetes?

A

Type 2 generally has enough insulin to prevent ketosis, however can develop under stress

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What syndrome can cause insulin resistance?

A

Cushings syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Treatment options mechanism for diabetes treatment?

A

Sulphonylureas: enhanced insulin secretion

Alpha-glucosidase inhibitors: reduced post-prandial hyperglycaemia

Metformin: reduced hepatic glucose concentration

Metformin and thiazolidinediones: reduced insulin resistance

Insulin: reduced hyperglycaemia

Incretin, sensitise B cells in pancreas to glucose, reducing the threshold for insulin release

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Possible causes of hyperglycaemia?

A

Insulin deficiency/increased catabolic hormones

Increased hepatic gluconeogenesis and glycogenolysis (unapposed glucagon)

Renal gluconeogenesis

insulin resistance increased

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Mechanisms for microvascular dysfunction in diabetes?

A

Endothelial cell dysfunction

Insulin resistance causes hyperlipidaemia

NO and vasodilator actions are impaired

Inflammation by Oxidative stress, cytokines, NO and adiponectin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Whats a hyperosmolar coma?

A

Extreme hyperglycaemia inducing coma, triggered by dehydration/infection/illness

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What in diabetes causes hypertriglyceridaemia?

A

LPL activity reduced = VLDLs and chylomicrons remaining in plasma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Main cause for diabetic ketoacidosis?

A

Switch to catabolic processes stimulated by glucagon leads to increased lipolysis and generation of ketones.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Symptoms and signs for ketoacidosis?

A

Increased thirst, polyuria

Dehydration, hypotension

Blurred vision

Nausea and vomiting

Can lead to coma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Why are counter regulatory hormone concentrations increased in diabetic ketoacidosis?

A

Low insulin leads to an early rise in glucagon

This leads to hyperglycaemia and diabetic ketoacidosis and dehydration this leads to the release of catecholamines and cortisol

Induces a vicious cycle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What exactly leads to the formation of ketones in diabetes?

A

Increased TG hydrolysis in adipose tissue leads to FA release, these circulate to the liver and are processed to produce Ketone bodies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Why does illness in diabetes lead to worsening of ketoacidosis?

A

Illness can lead to increases in catabolic hormones

Increasing the action of LPL

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How are ketone bodies disposed?

A

Most tissues use them

Oxidised and excreted through kidney and lungs

17
Q

How does the body try to compensate for the ketoacidosis?

A

Increased rate of deep breathing, using respiratory compensation (Kussmaul’s respiration)

18
Q

Why do you get ketoacidosis in type 2 diabetics but not in type 1?

A

In type 2 there is still insulin present, so acetyl CoA is converted to fatty acids instead of ketones.